Bringing added value to your studies
State-of-the-art electronic data source system allowing for direct data collection in electronic format, real-time data transfer, and remote monitoring, leading to greater efficiencies. SGS’s CPU has successfully passed multiple US Food & Drug Administration (US FDA) and Belgian FAMHP (Federal Agency for Medicines and Health Products) inspections during the last 5 years.
A strong team of (sub) Investigators (INV) and Clinical Research Coordinators (CRC), experienced in simple and complex studies, ensuring optimized safety management during the trial.
Our CPU’s extensive experience and expertise in early clinical trials can enhance your study experience.
Extensive and successful track record in early clinical development. On average, our CPU performs 30 studies every year with a population of healthy volunteers, special populations as well as patients, and uses a wide range of study design. A large bed capacity of 110 beds, of which 8 high care beds and 64 telemetry beds, spread over three wards, allowing for easy and flexible allocation.
On-site GMP production facility and in-house QP, allowing flexible dosing during the clinical trial. dedicated recruitment center, ensuring efficient subject enrolment and study delivery within timelines. Large recruitment capacity for healthy volunteers (> 13.000 active subjects registered in our database) by a
Fast study start-up due to low turnaround time of only 15 days for Regulatory Authority and Ethics Committee approval (low compared to most countries in Europe).
Technical resources and expertise to ensure excellent execution of complex procedures the bedside,
Dedicated therapeutic, pharmacology and clinical development experts assessing feasibility and ensuring smooth conduct of your study.
as well as optimal sample management throughout.
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